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Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy

INTRODUCTION: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no...

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Autores principales: Gouveia, Débora, Correia, Jéssica, Cardoso, Ana, Carvalho, Carla, Oliveira, Ana Catarina, Almeida, António, Gamboa, Óscar, Ribeiro, Lénio, Branquinho, Mariana, Sousa, Ana, Lopes, Bruna, Sousa, Patrícia, Moreira, Alícia, Coelho, André, Rêma, Alexandra, Alvites, Rui, Ferreira, António, Maurício, Ana Colette, Martins, Ângela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374290/
https://www.ncbi.nlm.nih.gov/pubmed/37520009
http://dx.doi.org/10.3389/fvets.2023.1192744
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author Gouveia, Débora
Correia, Jéssica
Cardoso, Ana
Carvalho, Carla
Oliveira, Ana Catarina
Almeida, António
Gamboa, Óscar
Ribeiro, Lénio
Branquinho, Mariana
Sousa, Ana
Lopes, Bruna
Sousa, Patrícia
Moreira, Alícia
Coelho, André
Rêma, Alexandra
Alvites, Rui
Ferreira, António
Maurício, Ana Colette
Martins, Ângela
author_facet Gouveia, Débora
Correia, Jéssica
Cardoso, Ana
Carvalho, Carla
Oliveira, Ana Catarina
Almeida, António
Gamboa, Óscar
Ribeiro, Lénio
Branquinho, Mariana
Sousa, Ana
Lopes, Bruna
Sousa, Patrícia
Moreira, Alícia
Coelho, André
Rêma, Alexandra
Alvites, Rui
Ferreira, António
Maurício, Ana Colette
Martins, Ângela
author_sort Gouveia, Débora
collection PubMed
description INTRODUCTION: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no specific treatment. Daily intensive rehabilitation showed survival time near 8 months but most animals are euthanized 6–12 months after clinical signs onset. METHODS: This prospective controlled blinded cohort clinical study aims to evaluate the neural regeneration response ability of DM dogs subjected to an intensive neurorehabilitation protocol with mesenchymal stem cells (MSCs) transplantation. In total, 13 non-ambulatory (OFS 6 or 8) dogs with homozygous genotype DM/DM and diagnosed by exclusion were included. All were allocated to the intensive neurorehabilitation with MSCs protocol (INSCP) group (n = 8) or to the ambulatory rehabilitation protocol (ARP) group (n = 5), which differ in regard to training intensity, modalities frequency, and MSCs transplantation. The INSCP group was hospitalized for 1 month (T0 to T1), followed by MSCs transplantation (T1) and a second month (T2), whereas the ARP group was under ambulatory treatment for the same 2 months. RESULTS: Survival mean time of total population was 375 days, with 438 days for the INSCP group and 274 for the ARP group, with a marked difference on the Kaplan–Meier survival analysis. When comparing the literature's results, there was also a clear difference in the one-sample t-test (p = 0.013) with an increase in time of approximately 70%. OFS classifications between groups at each time point were significantly different (p = 0.008) by the one-way ANOVA and the independent sample t-test. DISCUSSION: This INSCP showed to be safe, feasible, and a possibility for a long progression of DM dogs with quality of life and functional improvement. This study should be continued.
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spelling pubmed-103742902023-07-28 Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy Gouveia, Débora Correia, Jéssica Cardoso, Ana Carvalho, Carla Oliveira, Ana Catarina Almeida, António Gamboa, Óscar Ribeiro, Lénio Branquinho, Mariana Sousa, Ana Lopes, Bruna Sousa, Patrícia Moreira, Alícia Coelho, André Rêma, Alexandra Alvites, Rui Ferreira, António Maurício, Ana Colette Martins, Ângela Front Vet Sci Veterinary Science INTRODUCTION: Degenerative myelopathy (DM) is a neurodegenerative spinal cord disease with upper motor neurons, with progressive and chronic clinical signs, similar to amyotrophic lateral sclerosis (ALS). DM has a complex etiology mainly associated with SOD1 gene mutation and its toxic role, with no specific treatment. Daily intensive rehabilitation showed survival time near 8 months but most animals are euthanized 6–12 months after clinical signs onset. METHODS: This prospective controlled blinded cohort clinical study aims to evaluate the neural regeneration response ability of DM dogs subjected to an intensive neurorehabilitation protocol with mesenchymal stem cells (MSCs) transplantation. In total, 13 non-ambulatory (OFS 6 or 8) dogs with homozygous genotype DM/DM and diagnosed by exclusion were included. All were allocated to the intensive neurorehabilitation with MSCs protocol (INSCP) group (n = 8) or to the ambulatory rehabilitation protocol (ARP) group (n = 5), which differ in regard to training intensity, modalities frequency, and MSCs transplantation. The INSCP group was hospitalized for 1 month (T0 to T1), followed by MSCs transplantation (T1) and a second month (T2), whereas the ARP group was under ambulatory treatment for the same 2 months. RESULTS: Survival mean time of total population was 375 days, with 438 days for the INSCP group and 274 for the ARP group, with a marked difference on the Kaplan–Meier survival analysis. When comparing the literature's results, there was also a clear difference in the one-sample t-test (p = 0.013) with an increase in time of approximately 70%. OFS classifications between groups at each time point were significantly different (p = 0.008) by the one-way ANOVA and the independent sample t-test. DISCUSSION: This INSCP showed to be safe, feasible, and a possibility for a long progression of DM dogs with quality of life and functional improvement. This study should be continued. Frontiers Media S.A. 2023-07-13 /pmc/articles/PMC10374290/ /pubmed/37520009 http://dx.doi.org/10.3389/fvets.2023.1192744 Text en Copyright © 2023 Gouveia, Correia, Cardoso, Carvalho, Oliveira, Almeida, Gamboa, Ribeiro, Branquinho, Sousa, Lopes, Sousa, Moreira, Coelho, Rêma, Alvites, Ferreira, Maurício and Martins. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Veterinary Science
Gouveia, Débora
Correia, Jéssica
Cardoso, Ana
Carvalho, Carla
Oliveira, Ana Catarina
Almeida, António
Gamboa, Óscar
Ribeiro, Lénio
Branquinho, Mariana
Sousa, Ana
Lopes, Bruna
Sousa, Patrícia
Moreira, Alícia
Coelho, André
Rêma, Alexandra
Alvites, Rui
Ferreira, António
Maurício, Ana Colette
Martins, Ângela
Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
title Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
title_full Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
title_fullStr Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
title_full_unstemmed Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
title_short Intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
title_sort intensive neurorehabilitation and allogeneic stem cells transplantation in canine degenerative myelopathy
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374290/
https://www.ncbi.nlm.nih.gov/pubmed/37520009
http://dx.doi.org/10.3389/fvets.2023.1192744
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